Linked Data
dbSNP Id:
rs11554384
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99949733C>G , CM000666.2:g.99949733C>G | GRCh38 |
| NC_000004.11:g.100870890C>G , CM000666.1:g.100870890C>G | GRCh37 |
| NC_000004.10:g.101089913C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296417.6:c.11G>C MANE Select | ENSP00000296417.5:p.Gly4Ala | |
| ENST00000651623.1:c.11G>C | ENSP00000498935.1:p.Gly4Ala | |
| ENST00000296417.5:c.11G>C | ENSP00000296417.5:p.Gly4Ala | |
| ENST00000511203.1:n.567G>C | ||
| ENST00000511319.5:n.536G>C | ||
| ENST00000511348.1:n.196G>C | ||
| ENST00000527366.1:n.95G>C | ||
| ENST00000529158.5:n.60G>C | ||
| NM_002106.3:c.11G>C | NP_002097.1:p.Gly4Ala | |
| NM_002106.4:c.11G>C MANE Select | NP_002097.1:p.Gly4Ala |